Differential prevalence of Plasmodium infections and cryptic Plasmodium knowlesi malaria in humans in Thailand
- PMID: 19284284
- PMCID: PMC8817623
- DOI: 10.1086/597414
Differential prevalence of Plasmodium infections and cryptic Plasmodium knowlesi malaria in humans in Thailand
Abstract
Background: A case of human infection with Plasmodium knowlesi has been recently discovered in Thailand. To investigate the prevalence of this malaria species, a molecular-based survey was performed.
Methods: Blood samples from 1874 patients were tested for Plasmodium species by microscopy and nested polymerase chain reaction. P. knowlesi was characterized by sequencing the merozoite surface protein 1 gene (msp-1).
Results: Of all Plasmodium species identified, P. falciparum, P. vivax, P. malariae, P. ovale, and P. knowlesi contributed 43.52%, 68.08%, 1.37%, 1.03%, and 0.57%, respectively. Mixed-species infections were more common in northwestern and southwestern regions bordering Myanmar (23%-24%) than in eastern and southern areas (3%-5%). In northwestern and southwestern regions, mixed-species infections had a significantly higher prevalence in dry than in rainy seasons (P < .001). P. knowlesi was found in 10 patients, mostly from southern and southwestern areas-9 were coinfected with either P. falciparum or P. vivax. Most of the P. knowlesi Thai isolates were more closely related to isolates from macaques than to isolates from Sarawak patients. The msp-1 sequences of isolates from the same area of endemicity differed and possessed novel sequences, indicating genetic polymorphism in P. knowlesi infecting humans.
Conclusions: This survey highlights the widespread distribution of P. knowlesi in Thailand, albeit at low prevalence and mostly occurring as cryptic infections.
Conflict of interest statement
Potential conflicts of interest: No conflict
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Comment in
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Plasmodium knowlesi: finally being recognized.Collins WE, Barnwell JW. Collins WE, et al. J Infect Dis. 2009 Apr 15;199(8):1107-8. doi: 10.1086/597415. J Infect Dis. 2009. PMID: 19284287 No abstract available.
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